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Fexofenadine Hydrochloride
Fexofenadine Hydrochloride - 51079-529-20 - (fexofenadine hydrochloride)
Drug Information of Fexofenadine Hydrochloride
| Product NDC: | 51079-529 |
| Proprietary Name: | Fexofenadine Hydrochloride |
| Non Proprietary Name: | fexofenadine hydrochloride |
| Active Ingredient(s): | 60 mg/1 & nbsp; fexofenadine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Fexofenadine Hydrochloride
| Product NDC: | 51079-529 |
| Labeler Name: | UDL Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077081 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20101015 |
Package Information of Fexofenadine Hydrochloride
| Package NDC: | 51079-529-20 |
| Package Description: | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-529-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-529-01) |
NDC Information of Fexofenadine Hydrochloride
| NDC Code | 51079-529-20 |
| Proprietary Name | Fexofenadine Hydrochloride |
| Package Description | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-529-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-529-01) |
| Product NDC | 51079-529 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | fexofenadine hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20101015 |
| Marketing Category Name | ANDA |
| Labeler Name | UDL Laboratories, Inc. |
| Substance Name | FEXOFENADINE HYDROCHLORIDE |
| Strength Number | 60 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC] |
